Niacinamide 4% / Sodium Sulfacetamide Monohydrate 10%
Product Images NDC 72934-2156

3 FDA label images from Sincerus Florida, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Niacinamide 4% / Sodium Sulfacetamide Monohydrate 10% (NDC 72934-2156). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Ads (2 End)

Ads (2 End)
Side view of a white cylindrical container with a label showing usage directions and company contact information. The label advises applying the product topically, washing hands after use, and storing at controlled room temperature. It includes Sincerus Florida, LLC address and phone numbers for reporting adverse reactions.*
FDA Label Image

Sd (2156 2 Front)

Sd (2156 2 Front)
NIACINAMIDE 4% / SODIUM SULFACETAMIDE MONOHYDRATE 10% cream in a white cylindrical container with a label showing the product name, strength, cream form, and 30 gm quantity. The label also includes the NDC 72934-2156-2, the Sincerus Florida logo, and states that it is a compounded drug made in the USA.*
FDA Label Image

Sw (2156 2 Middle)

Sw (2156 2 Middle)
Close-up of a white cylindrical cream container label displaying active ingredients Niacinamide USP 4% and Sulfacetamide Sodium Monohydrate USP 10%. The label also lists inactive ingredients including glycerin, artificial rose water, krisgel 100, and sulfur precipitated USP. The label indicates a prescription-only product with batch and manufacturing dates shown as 01/01/1970.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.